| ID |
1 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000368089 |
| Start |
160041781:160041781(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.752T>C |
| AA Mutation |
p.Leu251Pro(p.L251P) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
2 |
| Mutation Consequence |
missense_variant |
| Transcription ID |
ENST00000368089 |
| Start |
160042325:160042325(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.208C>T |
| AA Mutation |
p.Leu70Phe(p.L70F) |
| Mutation Classification |
Missense_Mutation |
| Feature Type |
Transcript |
| ID |
3 |
| Mutation Consequence |
synonymous_variant |
| Transcription ID |
ENST00000368089 |
| Start |
160041507:160041507(version: GRCh38) |
| Mutation Type |
SNP |
| dbSNP_RS |
novel
|
| CDS Mutation |
c.1026C>T |
| Mutation Classification |
Silent |
| Feature Type |
Transcript |